Stowers Institute for Medical Research, Kansas City, MO, USA.
Department of Anatomy and Cell Biology, The University of Kansas School of Medicine, Kansas City, KS, USA.
Methods Mol Biol. 2022;2450:437-465. doi: 10.1007/978-1-0716-2172-1_23.
With a surprisingly complex genome and an ever-expanding genetic toolkit, the sea anemone Nematostella vectensis has become a powerful model system for the study of both development and whole-body regeneration. Here we provide the most current protocols for short-hairpin RNA (shRNA )-mediated gene knockdown and CRISPR/Cas9-targeted mutagenesis in this system. We further show that a simple Klenow reaction followed by in vitro transcription allows for the production of gene-specific shRNAs and single guide RNAs (sgRNAs) in a fast, affordable, and readily scalable manner. Together, shRNA knockdown and CRISPR/Cas9-targeted mutagenesis allow for rapid screens of gene function as well as the production of stable mutant lines that enable functional genetic analysis throughout the Nematostella life cycle.
海葵 Nematostella vectensis 拥有令人惊讶的复杂基因组和不断扩展的遗传工具包,已成为研究发育和整体再生的强大模式生物系统。在这里,我们提供了在该系统中使用短发夹 RNA(shRNA)介导的基因敲低和 CRISPR/Cas9 靶向诱变的最新方案。我们进一步表明,简单的 Klenow 反应后进行体外转录,可以快速、经济实惠且易于扩展的方式生成基因特异性 shRNA 和单指导 RNA(sgRNA)。shRNA 敲低和 CRISPR/Cas9 靶向诱变的结合可用于快速筛选基因功能,以及生成稳定的突变株,从而在 Nematostella 生命周期的整个过程中进行功能遗传分析。